Visitor Monitoring Drug History: BUPROPION HYDROCHLORIDE
 
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Label and Approval History

Drug Name: BUPROPION HYDROCHLORIDE
FDA Application No: (ANDA) 075932
Active Ingredient(s): BUPROPION HYDROCHLORIDE
Company: SANDOZ
 
Label History
 
Labels are not available on this site for BUPROPION HYDROCHLORIDE, (ANDA) 075932
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
6/22/2005 013Supplement  
6/22/2005 012Supplement  
6/22/2005 005Supplement  
6/22/2005 004Supplement  
3/22/2004 002Supplement Letter
Review 
3/22/2004 001Supplement Letter
Review 
1/24/2002 000Tentative Approval Letter
Review
Other Important Information from FDA 
11/25/2003 000Approval Letter
Review
Other Important Information from FDA 
 
Therapeutic Equivalents
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